Saturday, October 29, 2016
Wednesday, October 26, 2016
Just Like A Snake
Temperature particles provide continuous spectra in the ultraviolet, the infrared, and visible range ("Lemmings Over The Cliff..." dated 18 May 2016). Temperature particles could also be responsible for smell and taste, that fresh vegetable and food taste bland after they have been stored in cool temperature. The coolness of negative temperature particles neutralizes positive temperature particle and takes the taste/smell away.
So, if you are able to isolate temperature particles, give positive temperature particles a good lick and varies its amount as you do so. It is likely that a combination of positive and negative temperature particles in succession provide a unique favor to foodstuff.
Just like a snake tasting the air with its tongue is seeing in infrared.
So, if you are able to isolate temperature particles, give positive temperature particles a good lick and varies its amount as you do so. It is likely that a combination of positive and negative temperature particles in succession provide a unique favor to foodstuff.
Just like a snake tasting the air with its tongue is seeing in infrared.
Tuesday, October 25, 2016
Absorbed!
But a plot of (x^(1/3)-a^(1/3))/((a*x)^(1/3))-ln((x/a)^(1/3)) for a =1 to 7 is,
All absorption lines! A plot of 1/a^2-1/x^2 for a =1 to 7 gives,
which indicates,
h≠c5πaψcmψ
on the basis that Rydberg formula is correct.
What is h?
All absorption lines! A plot of 1/a^2-1/x^2 for a =1 to 7 gives,
which indicates,
h≠c5πaψcmψ
on the basis that Rydberg formula is correct.
What is h?
It Is Just Nice To Look At
Hei, from the previous post "A Deep Dark Secret" dated 25 Oct 2016,
F=25mψa2ψ(c2πaψ)21aψ
instead,
Fρ=25mψa2ψ(c2πaψ)21aψ
since we are dealing with ψ and it is force density all along, mψ=m is mass density, a constant. So,
Fρn1=25mψa2ψn1(c2πaψn1)21aψn1
then
Fρn1=110π2mψc2aψn1
W1→2=∫aψn2aψn1Fρndaψ
W1→2=∫n2n1Fρnd(3√n.aψc)
W1→2=mψc210π2∫n2n113√n.d3√n
W1→2=mψc210π2[ln(3√n2)−ln(3√n1)]=mψc210π2ln(3√n23√n1)
W1→2=mψc210π2ln(aψn2aψn1)
Which is somehow very satisfying, irrespective of all and any maths and logic blunders. It is so nice I took a second look. Since,
fc=c2πaψc
the expression suggests,
h=c5πaψcmψ
which would be a constant for a given particle. Nice!
A plot of ln((n_2/n_1)^(1/3)) for n_1 = 1 to 7 is given below,
As aψn1→aψn2, there is an release of energy as the particle grows bigger. W1→2 requires energy and reduces the amount of energy released.
The most energy required from a transition from n1=1 results in a absorption line.
Big particle with less energy in ψ is counter-intuitive. Big particle has ψ going around its circumference at lower frequency, given that ψ has a constant speed, light speed.
But a big particle contains a small particle!?
A big particle has more extensive ψ but its ψ has less energy when we take reference at the circumference/surface of the particle.
v=rω
All inner ψ have lower speed, when they do not slide along each other. ψ outside from the center of the particle need to move faster; the fastest of which is light speed.
F=25mψa2ψ(c2πaψ)21aψ
instead,
Fρ=25mψa2ψ(c2πaψ)21aψ
since we are dealing with ψ and it is force density all along, mψ=m is mass density, a constant. So,
Fρn1=25mψa2ψn1(c2πaψn1)21aψn1
then
and similarly,
Fρn2=110π2mψc2aψn2
In general,
Fρn=110π2mψc2aψc.13√n
since,
1n=(aψcaψn)3
as such,
In general,
Fρn=110π2mψc2aψc.13√n
since,
1n=(aψcaψn)3
as such,
W1→2=∫aψn2aψn1Fρndaψ
W1→2=∫n2n1Fρnd(3√n.aψc)
W1→2=mψc210π2∫n2n113√n.d3√n
and
W1→2=mψc210π2[ln(3√n2)−ln(3√n1)]=mψc210π2ln(3√n23√n1)
W1→2=mψc210π2ln(aψn2aψn1)
Which is somehow very satisfying, irrespective of all and any maths and logic blunders. It is so nice I took a second look. Since,
fc=c2πaψc
the expression suggests,
h=c5πaψcmψ
which would be a constant for a given particle. Nice!
A plot of ln((n_2/n_1)^(1/3)) for n_1 = 1 to 7 is given below,
As aψn1→aψn2, there is an release of energy as the particle grows bigger. W1→2 requires energy and reduces the amount of energy released.
The most energy required from a transition from n1=1 results in a absorption line.
Big particle with less energy in ψ is counter-intuitive. Big particle has ψ going around its circumference at lower frequency, given that ψ has a constant speed, light speed.
But a big particle contains a small particle!?
A big particle has more extensive ψ but its ψ has less energy when we take reference at the circumference/surface of the particle.
v=rω
All inner ψ have lower speed, when they do not slide along each other. ψ outside from the center of the particle need to move faster; the fastest of which is light speed.
Monday, October 24, 2016
A Deep Dark Secret
Consider the force holding ψ in circular motion,
L=Iω
F=Lωr
scale by r, as the further from the center the less L has to turn,
F=Iω2r
In the case of a point mass, m in circular motion with velocity v, in circle of radius of r,
F=mr2(vr)2.1r=mv2r
where I=mr2 and ω=vr in radian per second. Which is as expected.
In this case of a sphere of ψ,
F=25mψa2ψ(c2πaψ)2.1aψ
where ω=v2πaψ in per second.
mψ=ρψ.43πa3ψ
F=430πc2ρψ.a2ψ
W1→2=∫aψn2aψn1Fdaψ
If we assume that, ρψ∝ψ.
For,
aψn1>aψπ and aψn2>aψπ
ψ=ψπ=constant
We have,
W1→2=490πc2ρψ[a3ψn2−a3ψn1]
W1→2=490πc2ρψa3ψc[n2−n1]
which is just as wrong as the other expressions derived previously.
For,
aψn1<aψπ
aψn2<aψπ
W1→2=∫aψn2aψn1Fdaψ=430πc2∫aψn2aψn1ρψ.a2ψdaψ
From the post "Not Quite The Same Newtonian Field" dated 23 Nov 2014,
ψ=−i2mc2ln(cosh(G√2mc2(x−xz)))+c
ψ=−2mc2ln(cosh(G√2mc2(aψ)))
under the assumption, ρψ∝ψ
ρψ=A.ψ
We have,
W1→2=A.830πmc2∫aψn2aψn1−a2ψln(cosh(G√2mc2(aψ)))daψ
At last, inevitably the ugly bride meets the in-laws ...
What is m? This was a problem since Fρ or F, the force density was written down. A force has to act on some mass. If force density acts on mass density then,
ρψ=m
then ψ=f(ρψ), given ρψ,
ψ=−2ρψc2ln(cosh(G√2ρψc2(aψ)))
from which we solve for ρψ given ψ. Which make sense because W1→2 is moving ψ about, we must know the amount of ψ in question to calculate W1→2.
But does energy density has mass density? Does energy has mass?
This path does not provide an easy answer to W1→2 as Ln1→Ln2. W1→2 might be similar to Rydberg formula,
1λ=RH(1n21−1n22)
A new passport and a ticket to nowhere...you asked for it!
L=Iω
F=Lωr
scale by r, as the further from the center the less L has to turn,
F=Iω2r
In the case of a point mass, m in circular motion with velocity v, in circle of radius of r,
F=mr2(vr)2.1r=mv2r
where I=mr2 and ω=vr in radian per second. Which is as expected.
In this case of a sphere of ψ,
F=25mψa2ψ(c2πaψ)2.1aψ
where ω=v2πaψ in per second.
mψ=ρψ.43πa3ψ
F=430πc2ρψ.a2ψ
W1→2=∫aψn2aψn1Fdaψ
If we assume that, ρψ∝ψ.
For,
aψn1>aψπ and aψn2>aψπ
ψ=ψπ=constant
We have,
W1→2=490πc2ρψ[a3ψn2−a3ψn1]
W1→2=490πc2ρψa3ψc[n2−n1]
which is just as wrong as the other expressions derived previously.
For,
aψn1<aψπ
aψn2<aψπ
W1→2=∫aψn2aψn1Fdaψ=430πc2∫aψn2aψn1ρψ.a2ψdaψ
From the post "Not Quite The Same Newtonian Field" dated 23 Nov 2014,
ψ=−2mc2ln(cosh(G√2mc2(aψ)))
under the assumption, ρψ∝ψ
ρψ=A.ψ
We have,
W1→2=A.830πmc2∫aψn2aψn1−a2ψln(cosh(G√2mc2(aψ)))daψ
At last, inevitably the ugly bride meets the in-laws ...
What is m? This was a problem since Fρ or F, the force density was written down. A force has to act on some mass. If force density acts on mass density then,
ρψ=m
then ψ=f(ρψ), given ρψ,
ψ=−2ρψc2ln(cosh(G√2ρψc2(aψ)))
from which we solve for ρψ given ψ. Which make sense because W1→2 is moving ψ about, we must know the amount of ψ in question to calculate W1→2.
But does energy density has mass density? Does energy has mass?
This path does not provide an easy answer to W1→2 as Ln1→Ln2. W1→2 might be similar to Rydberg formula,
1λ=RH(1n21−1n22)
A new passport and a ticket to nowhere...you asked for it!
Sunday, October 23, 2016
Not Orbits!
There is no orbits, ψ is held by Fρ the force density. Moving ψ away from the center of the particle act against Fρ or ∫Fρdr.
There is no charge particle holding another oppositely charged particle, and no field between the oppositely charged particles, along which potential energy changes.
There is no charge particle holding another oppositely charged particle, and no field between the oppositely charged particles, along which potential energy changes.
Saturday, October 22, 2016
Adjusting for Bohr - Angular Momentum
The expression,
ΔE2→1=h.fψc(3√n2−3√n13√n1n2−n2o2−n2o1(no1no2)2)
from the post "Particles In Orbits" dated 18 Oct 2016, with ni=noi=i,
ΔE2→1=h.fψc(3√n2−3√n13√n1n2−n22−n21(n1n2)2)
The term,
3√n2−3√n13√n1n2
is due to the difference in potential energy associated with the spin of ψ with n1 and n2, at aψn1 and aψn2, respectively, and the term,
n22−n21(n1n2)2
is the change in energy as momentum changes due to a change in n, assuming that the particles after coalescence/separation are still at light speed.
Let's formulate the change in energy as per Bohr model due to a quantized change in momentum. Since n is an integer, the change in momentum is equally spaced and so if Ln1 is the momentum of the
KEn1=L2n12m1
KEn2=L2n22m2
the change in KE is
ΔKE=KEn2−KEn1=−ΔPE
ΔPE=L2n12m1−L2n22m2
since we know that the change in momentum is entirely due to a change in n. For a particle spinning at light speed c,
Ln2=25m2a2ψn2.c2πaψn2=c5πm2aψn2
Ln1=25m1a2ψn1.c2πaψn1=c5πm1aψn1
where Ini=25mi.a2ψni is the moment of inertia of a sphere of radius aψni. So,
ΔPE=m1(aψn1c)250π2−m2(aψn2c)250π2=c250π2(m1a2ψn1−m2a2ψn2)
As particle of radius aψn1 is made up of n1 basic particle of radius aψc, n=1
1n1=(aψcaψn1)3, aψn2=3√n2aψc
and particle of radius aψn2 is made up of n2 basic particle of radius aψc, n=1
1n2=(aψcaψn2)3, aψn1=3√n1aψc
Since we have assumed that the volume of the particles are conserved and their density is a constant,
m1=n1mc
m2=n2mc
So after substituting for mi,
ΔPE=mcc250π2(n1a2ψn1−n2a2ψn2)
ΔPE=mcc250π2(n1(3√n1aψc)2−n2(3√n2aψc)2)
ΔPE=mcc250π2a2ψc(n5/31−n5/32)
Lc=25mca2ψc.c2πaψc
ΔPE=L2c2mc(n5/31−n5/32)
What happened to 1n21−1n22? The above expression is the change in KE required for the specified change in momentum, it is not the associated change in energy level of the particle in its field.
Consider again,
Ln2=25m2a2ψn2.c2πaψn2=c5πm2aψn2
Ln2Ln1=m2m1.aψn2aψn1
Ln2Ln1=n2n1.3√n2n1=(n2n1)4/3
Which is not Ln1Ln2=n1n2 as in Bohr model of
L=nℏ
And if we follow through the derivation for the energy difference between two energy levels, n1 and n2 we have,
EB=RE(1(n4/31)2−1(n4/32)2)=RE(1n2.6671−1n2.6672)
this does not effect the first term, 3√n2−3√n13√n1n2=13√n1−13√n2 associated with the decrease in potential energy of the system in circular motion, as ψ move from n1→n2.
EB derived above is the potential energy change in the field (E∝1r) that accompanies a change in the angular momentum of ψ as the energy level transition n1→n2 occurs. EB is recovered from the amount of potential energy associated with the system in circular motion, released.
C=3√n2−3√n13√n1n2−n2.6672−n2.6671(n1n2)2.667
Does a system in circular motion have potential energy h.f in addition to the system KE as quantified by its angular momentum? The work done field against the force −∂ψ∂r as ψ moves away from the center along a radial line, is strictly not ∝1r2 but, the Newtonian F,
F∝−∫Fρdr
F∝−ln(cosh(r))
E∝−∫ln(cosh(r))dr
and things get very difficult.
A series plot of ((x)^(1/3)-(a)^(1/3))/(a*x)^(1/3)-((x)^(2.667)-(a)^(2.667))/(a*x)^2.667 for a =1 to 6 is given below,
where the plots for n1=2 and n1=3 is almost coincidental.
After adjusting for 2→2.667, the plots are essentially the same except that the overlapping plots are not n1=2 and n1=5 but n1=2 and n1=3.
It seems that n1=2 and n1=3 are degenerate, instead.
The important points are: a pair of degenerate plots (n1=2 and n1=3) very close together occurs naturally, that the plot for n1=1 is an absorption line and the rest of the plots n1≥2 are the emission background.
Good night.
Note: The potential energy of a ball in circular motion held by a spring, is the energy stored in the spring as the spring stretches to provide for a centripetal force. It is clear in this case, that the KE of the ball, (equivalently stated as angular momentum) is a separate issue from the potential energy stored in the spring. The energy required to increase the ball's KE1→KE2 is not the same as the energy required to stretch the spring further as the ball accelerates from KE1→KE2.
It could be that 3√n2−3√n13√n1n2 defines the energy change needed at the perimeter, aψn2 and −n2.6672−n2.6671(n1n2)2.667 is the change in energy along a radial line from n1 to n2.
Note: Positive is emission line, and negative is absorption line
ΔE2→1=h.fψc(3√n2−3√n13√n1n2−n2o2−n2o1(no1no2)2)
from the post "Particles In Orbits" dated 18 Oct 2016, with ni=noi=i,
ΔE2→1=h.fψc(3√n2−3√n13√n1n2−n22−n21(n1n2)2)
is ARBITRARY. It is the result of comparing the leading constant to Planck relation E=h.f
3√n2−3√n13√n1n2
is due to the difference in potential energy associated with the spin of ψ with n1 and n2, at aψn1 and aψn2, respectively, and the term,
n22−n21(n1n2)2
is the change in energy as momentum changes due to a change in n, assuming that the particles after coalescence/separation are still at light speed.
Let's formulate the change in energy as per Bohr model due to a quantized change in momentum. Since n is an integer, the change in momentum is equally spaced and so if Ln1 is the momentum of the
KEn1=L2n12m1
KEn2=L2n22m2
the change in KE is
ΔKE=KEn2−KEn1=−ΔPE
ΔPE=L2n12m1−L2n22m2
since we know that the change in momentum is entirely due to a change in n. For a particle spinning at light speed c,
Ln2=25m2a2ψn2.c2πaψn2=c5πm2aψn2
Ln1=25m1a2ψn1.c2πaψn1=c5πm1aψn1
where Ini=25mi.a2ψni is the moment of inertia of a sphere of radius aψni. So,
ΔPE=m1(aψn1c)250π2−m2(aψn2c)250π2=c250π2(m1a2ψn1−m2a2ψn2)
As particle of radius aψn1 is made up of n1 basic particle of radius aψc, n=1
1n1=(aψcaψn1)3, aψn2=3√n2aψc
and particle of radius aψn2 is made up of n2 basic particle of radius aψc, n=1
1n2=(aψcaψn2)3, aψn1=3√n1aψc
m1=n1mc
m2=n2mc
So after substituting for mi,
ΔPE=mcc250π2(n1a2ψn1−n2a2ψn2)
And after substituting for aψi,
ΔPE=mcc250π2(n1(3√n1aψc)2−n2(3√n2aψc)2)
ΔPE=mcc250π2a2ψc(n5/31−n5/32)
Lc=25mca2ψc.c2πaψc
ΔPE=L2c2mc(n5/31−n5/32)
What happened to 1n21−1n22? The above expression is the change in KE required for the specified change in momentum, it is not the associated change in energy level of the particle in its field.
Consider again,
Ln2=25m2a2ψn2.c2πaψn2=c5πm2aψn2
Ln2Ln1=m2m1.aψn2aψn1
Ln2Ln1=n2n1.3√n2n1=(n2n1)4/3
Which is not Ln1Ln2=n1n2 as in Bohr model of
L=nℏ
And if we follow through the derivation for the energy difference between two energy levels, n1 and n2 we have,
EB=RE(1(n4/31)2−1(n4/32)2)=RE(1n2.6671−1n2.6672)
this does not effect the first term, 3√n2−3√n13√n1n2=13√n1−13√n2 associated with the decrease in potential energy of the system in circular motion, as ψ move from n1→n2.
EB derived above is the potential energy change in the field (E∝1r) that accompanies a change in the angular momentum of ψ as the energy level transition n1→n2 occurs. EB is recovered from the amount of potential energy associated with the system in circular motion, released.
C=3√n2−3√n13√n1n2−n2.6672−n2.6671(n1n2)2.667
Does a system in circular motion have potential energy h.f in addition to the system KE as quantified by its angular momentum? The work done field against the force −∂ψ∂r as ψ moves away from the center along a radial line, is strictly not ∝1r2 but, the Newtonian F,
F∝−∫Fρdr
F∝−ln(cosh(r))
E∝−∫ln(cosh(r))dr
and things get very difficult.
A series plot of ((x)^(1/3)-(a)^(1/3))/(a*x)^(1/3)-((x)^(2.667)-(a)^(2.667))/(a*x)^2.667 for a =1 to 6 is given below,
where the plots for n1=2 and n1=3 is almost coincidental.
After adjusting for 2→2.667, the plots are essentially the same except that the overlapping plots are not n1=2 and n1=5 but n1=2 and n1=3.
It seems that n1=2 and n1=3 are degenerate, instead.
The important points are: a pair of degenerate plots (n1=2 and n1=3) very close together occurs naturally, that the plot for n1=1 is an absorption line and the rest of the plots n1≥2 are the emission background.
Good night.
Note: The potential energy of a ball in circular motion held by a spring, is the energy stored in the spring as the spring stretches to provide for a centripetal force. It is clear in this case, that the KE of the ball, (equivalently stated as angular momentum) is a separate issue from the potential energy stored in the spring. The energy required to increase the ball's KE1→KE2 is not the same as the energy required to stretch the spring further as the ball accelerates from KE1→KE2.
It could be that 3√n2−3√n13√n1n2 defines the energy change needed at the perimeter, aψn2 and −n2.6672−n2.6671(n1n2)2.667 is the change in energy along a radial line from n1 to n2.
Note: Positive is emission line, and negative is absorption line
Wednesday, October 19, 2016
How Big To Be?
The emission spectrum is continuous with n2 large. As the total energy of the system increases with high electric field or high temperature, n1 can take on smaller values. The absorption lines with n1=1 are distinctive against the background of continuous emission. How small is n1 to be?
n1=1
In order to generate a continuous emission spectrum, how big is n2 to be?
n2=nlarge>>77
How to make n2 big? If n2 is spinning about the center of the particle, will n2 be big? The centripetal force acting against a pinch force that pull ψ away from the particle will allow more ψ to attach itself to the particle and allows n2 to increase.
Maybe...
n1=1
In order to generate a continuous emission spectrum, how big is n2 to be?
n2=nlarge>>77
How to make n2 big? If n2 is spinning about the center of the particle, will n2 be big? The centripetal force acting against a pinch force that pull ψ away from the particle will allow more ψ to attach itself to the particle and allows n2 to increase.
Maybe...
Tuesday, October 18, 2016
Electrons May Not Be Involved!
With,
C=3√n2−3√n13√n1n2−n22−n21(n1n2)2
Could it be that because the spectrum observations are conducted at high temperature,
3√n2−3√n13√n1n2
is due to temperature particles. And,
n22−n21(n1n2)2
orbiting particles not necessarily electrons.
C=CT+CB
where CT is due to the energy density ψ of interacting temperature particles and CB due to Bohr model not necessarily of electrons, with quantized momenta.
Temperature particles orbiting around electron orbits that in resonance produce the infrared spectrum and the ultraviolet spectrum was proposed previously "Lemmings Over The Cliff..." dated 18 May 2016. Spectra lines in the visible spectrum will come from transitions between energy levels in the ultraviolet spectrum.
Electrons may not be involved! Unless the observations are also conducted in the presence of a high electric field, electron are not affected. If this is the case, temperature should be raised without the use of an electric field. Within the confines of the experiment, there should be only one strong field affecting one type of particles.
Let electrons not be involved. Maybe then spectra lines can be indicative of the existence of temperature particles in orbit around electron orbits as proposed in the post "Capturing T+ Particles" dated 15 May 2016.
In which case, electron ionization energies has no direct relation with spectra lines (due to temperature particles), not even in the simplest model of Hydrogen atoms.
Have a nice day...
C=3√n2−3√n13√n1n2−n22−n21(n1n2)2
Could it be that because the spectrum observations are conducted at high temperature,
3√n2−3√n13√n1n2
is due to temperature particles. And,
n22−n21(n1n2)2
orbiting particles not necessarily electrons.
C=CT+CB
where CT is due to the energy density ψ of interacting temperature particles and CB due to Bohr model not necessarily of electrons, with quantized momenta.
Temperature particles orbiting around electron orbits that in resonance produce the infrared spectrum and the ultraviolet spectrum was proposed previously "Lemmings Over The Cliff..." dated 18 May 2016. Spectra lines in the visible spectrum will come from transitions between energy levels in the ultraviolet spectrum.
Electrons may not be involved! Unless the observations are also conducted in the presence of a high electric field, electron are not affected. If this is the case, temperature should be raised without the use of an electric field. Within the confines of the experiment, there should be only one strong field affecting one type of particles.
Let electrons not be involved. Maybe then spectra lines can be indicative of the existence of temperature particles in orbit around electron orbits as proposed in the post "Capturing T+ Particles" dated 15 May 2016.
In which case, electron ionization energies has no direct relation with spectra lines (due to temperature particles), not even in the simplest model of Hydrogen atoms.
Have a nice day...
When Wrong Is Right
I know...
Emission spectrum is taken to be the complement of the absorption spectrum.
If all energy transitions have its complement then, they should all cancel. Dark lines should not be visible and the background emission spectrum against which they appears must also be accounted for. Ambient light or indirect illumination alone does not generate the background emission spectrum.
Emission spectrum in this blog refers to the backdrop upon which the dark absorption lines appears.
Redefining everything to be right...When wrong is right, what's left? Right??
Eliminate all indirect illumination, does fine gaps appears in the background emission spectrum?
Wrong does not make left right, it just leaves behind more questions... More questions are what's left!
Emission spectrum is taken to be the complement of the absorption spectrum.
If all energy transitions have its complement then, they should all cancel. Dark lines should not be visible and the background emission spectrum against which they appears must also be accounted for. Ambient light or indirect illumination alone does not generate the background emission spectrum.
Emission spectrum in this blog refers to the backdrop upon which the dark absorption lines appears.
Redefining everything to be right...When wrong is right, what's left? Right??
Eliminate all indirect illumination, does fine gaps appears in the background emission spectrum?
Wrong does not make left right, it just leaves behind more questions... More questions are what's left!
What "It"?
Given,
C=3√n2−3√n13√n1n2−n22−n21(n1n2)2
when n2<n1, for absorption lines, n1↔n2,
D=n22−n21(n1n2)2−3√n2−3√n13√n1n2=−C
And so we can expect the spectra line n1→2 to cancel the reverse spectra line n2→1.
For the sake of it....
C=3√n2−3√n13√n1n2−n22−n21(n1n2)2
when n2<n1, for absorption lines, n1↔n2,
D=n22−n21(n1n2)2−3√n2−3√n13√n1n2=−C
And so we can expect the spectra line n1→2 to cancel the reverse spectra line n2→1.
For the sake of it....
The Total Picture
Why is emission that occurs at the same time as absorption lines almost continuous, whereas absorption lines are spaced far apart?
For each value of n2, we have an absorption line. All possible values of n2 generates an absorption series.
With many n1=1 plots corresponding to different allowable energy states, we have a number of absorption series that depict such plausible energy states.
Which is confusing because of the one added level of indirection. For example,
n1=1 for n=1
n1=1 for n=2
and
n1=1 for n=3
where the lowest energy level of a particle of two constituent basic particles is different (higher) than the lowest energy of a particle with three constituent basic particles.
What happened to ni=noi=i?
This expression considers the lowest (first, n1=1) energy level in a set of all particle sizes (all n).
Energy transitions occur for a particle given its number of constituent basic particle size n with a particular first/lowest energy state. The lowest energy level n1, given n is an absorption series given all values of n2. Across all possible values of n1 as particle n size changes, we have different absorption series.
And the question was, why is it an absorption line? Which leads to the question, are there fine gaps in the background emission spectrum?
Note: In the plot above n1=1 is indicative of the lowest energy level of a particular n. Given all values of n2, n1=1 for a particular n generates a absorption series. When n is higher n1=1 is lower, with less energy. Different n, generates different spectra series.
For each value of n2, we have an absorption line. All possible values of n2 generates an absorption series.
With many n1=1 plots corresponding to different allowable energy states, we have a number of absorption series that depict such plausible energy states.
Which is confusing because of the one added level of indirection. For example,
n1=1 for n=1
n1=1 for n=2
and
n1=1 for n=3
where the lowest energy level of a particle of two constituent basic particles is different (higher) than the lowest energy of a particle with three constituent basic particles.
What happened to ni=noi=i?
This expression considers the lowest (first, n1=1) energy level in a set of all particle sizes (all n).
Energy transitions occur for a particle given its number of constituent basic particle size n with a particular first/lowest energy state. The lowest energy level n1, given n is an absorption series given all values of n2. Across all possible values of n1 as particle n size changes, we have different absorption series.
And the question was, why is it an absorption line? Which leads to the question, are there fine gaps in the background emission spectrum?
Note: In the plot above n1=1 is indicative of the lowest energy level of a particular n. Given all values of n2, n1=1 for a particular n generates a absorption series. When n is higher n1=1 is lower, with less energy. Different n, generates different spectra series.
Shifty Spectra
Given equal probabilities that an emission or absorption occurs at all energy levels to all energy levels, why does not −E1→n, an emission line and En→1, where n2=n1, an absorption line, cancels?
When n2<n1, emission plots become absorption plots but the single absorption plot does not become an emission plot. For the case of n1=1 there cannot be a lower n2, so there is no emission lines from n1 to a lower energy level. This does not mean that there is no emission lines that would cancel the absorption lines from n1=1. A transition E2→1 would generate a emission line that cancels the absorption line of E1→2.
Do the forward transition and its the reversed transition cancels? Only with numerical calculations can tell.
but we see that,
because the emission plots are not parallel for values of n2 smaller than n2 at the minimum point. And in the following case its is not possible to tell graphically whether the forward transition and its reversed transition cancels,
Notice that E2→3 is an emission line and E3→2 is an absorption line. All transitions to the left of the final energy state plot minimum point n2min have the opposite sign. The corresponding reversed transition is at the minimum point and move downwards vertically to the final energy state.
It is also noted that for the plot n1=5 another zero x-axis intercept occurs at n2=2. And that for the plot n1=2 another zero x-axis intercept occurs at n2=5.
Both plots are coincidental. This suggests that moving from n1=2 to n2=5 and in reverse, requires no net energy. In moving from n1= to n2=5, the loss in energy due to a decrease in aψ at n2=5 is made up for by the increase in orbital energy there, and vice versa.
It is possible that there is an energy gradient as the spectra line observations are being made. When energy of the system is increasing, small particles tend to form and n1>n2. When energy of the system is decreasing, big particles tend to form on separation after a collision and n1<n2. In this way, n1≠n2 and the emission lines are not coincidental with the absorption lines. Emission and absorption that cancel do not occur with equal probability.
Which means, with no energy input to the system, the spectra line would disappear, but a different sets of lines reappears as the system cools.
Note: The difference between ΔE1→2 and E1→2 is the overall change in energy state as demarcated by the definition of one single process and one energy state change of many in a more prolonged process.
In the case where separation follows coalescence,
ΔE1→2≠h.f
instead there are both an emission line,
E1→n
and an absorption line,
En→2
As the small particle grows bigger its energy drops due to a larger aψ.
When n2<n1, emission plots become absorption plots but the single absorption plot does not become an emission plot. For the case of n1=1 there cannot be a lower n2, so there is no emission lines from n1 to a lower energy level. This does not mean that there is no emission lines that would cancel the absorption lines from n1=1. A transition E2→1 would generate a emission line that cancels the absorption line of E1→2.
Do the forward transition and its the reversed transition cancels? Only with numerical calculations can tell.
but we see that,
because the emission plots are not parallel for values of n2 smaller than n2 at the minimum point. And in the following case its is not possible to tell graphically whether the forward transition and its reversed transition cancels,
Notice that E2→3 is an emission line and E3→2 is an absorption line. All transitions to the left of the final energy state plot minimum point n2min have the opposite sign. The corresponding reversed transition is at the minimum point and move downwards vertically to the final energy state.
It is also noted that for the plot n1=5 another zero x-axis intercept occurs at n2=2. And that for the plot n1=2 another zero x-axis intercept occurs at n2=5.
Both plots are coincidental. This suggests that moving from n1=2 to n2=5 and in reverse, requires no net energy. In moving from n1= to n2=5, the loss in energy due to a decrease in aψ at n2=5 is made up for by the increase in orbital energy there, and vice versa.
It is possible that there is an energy gradient as the spectra line observations are being made. When energy of the system is increasing, small particles tend to form and n1>n2. When energy of the system is decreasing, big particles tend to form on separation after a collision and n1<n2. In this way, n1≠n2 and the emission lines are not coincidental with the absorption lines. Emission and absorption that cancel do not occur with equal probability.
Which means, with no energy input to the system, the spectra line would disappear, but a different sets of lines reappears as the system cools.
Note: The difference between ΔE1→2 and E1→2 is the overall change in energy state as demarcated by the definition of one single process and one energy state change of many in a more prolonged process.
In the case where separation follows coalescence,
ΔE1→2≠h.f
instead there are both an emission line,
E1→n
and an absorption line,
En→2
As the small particle grows bigger its energy drops due to a larger aψ.
We All Have Our Say, Give And Take
We can do away with the notion of colliding atoms and think of the high energy experimental conditions as being conducive to the formation of small particles,
In the top most diagram, a small particle passes through a big particle with energy transitions −E1→n and En→2 occurring, on entering the big particle and on leaving the big particle. Both emission and absorption of energy occur in the same process. The overall change in energy state is,
ΔE1→2=En→2−E1→n
but −E1→n is energy emission and En→2 is energy absorption.
In the middle diagram, the small particle coalesce with the big particle and the lowest energy level attained is,
n=nlarge+n1
and the resulting bigger particle subsequently breaks into n−n2 and n2 particles where n2≠n1. This differ from the toppest case where n≠nlarge+n1 but simply n>n1. The small particle passing through the big particle retains its distinctiveness because of its high momentum. These two diagrams provide two scenarios as to what happened to the small particle inside the big particle. In both cases a subsequent departure follows coalescence.
The third diagram shows a simple coalescence without a subsequent separation. Only one singular energy emission occurs as n1→nlarge+1.
All three process occur simultaneously. Emissions form the colored background against which dark absorption lines show up in contrast.
Have a nice day.
Note: This discussion is of all n1, not just n1=1. The case of n1=1 generates an absorption series given the two processes involved; changing aψ and changing orbital energy level as according to Bohr model.
In the top most diagram, a small particle passes through a big particle with energy transitions −E1→n and En→2 occurring, on entering the big particle and on leaving the big particle. Both emission and absorption of energy occur in the same process. The overall change in energy state is,
ΔE1→2=En→2−E1→n
but −E1→n is energy emission and En→2 is energy absorption.
In the middle diagram, the small particle coalesce with the big particle and the lowest energy level attained is,
n=nlarge+n1
and the resulting bigger particle subsequently breaks into n−n2 and n2 particles where n2≠n1. This differ from the toppest case where n≠nlarge+n1 but simply n>n1. The small particle passing through the big particle retains its distinctiveness because of its high momentum. These two diagrams provide two scenarios as to what happened to the small particle inside the big particle. In both cases a subsequent departure follows coalescence.
The third diagram shows a simple coalescence without a subsequent separation. Only one singular energy emission occurs as n1→nlarge+1.
All three process occur simultaneously. Emissions form the colored background against which dark absorption lines show up in contrast.
Have a nice day.
Note: This discussion is of all n1, not just n1=1. The case of n1=1 generates an absorption series given the two processes involved; changing aψ and changing orbital energy level as according to Bohr model.
Speculating While Others Sleep...
Continued from the previous post "Particles In Orbits" dated 18 Oct 2016,
n1=no1=1
where the lowest energy level coincides with the smallest particle. In general,
ni=noi=i
if we argue that given light speed a constant, angular momentum at light speed increases proportionally with the number of constituent basic particle n. This makes noi from Bohr model coincidental with ni, the number of constituent basic particles.
Which brings us to the emission plots n1=2 and n1=5,
When experimental conditions are such that ni≠noi, these two plots will split and emerge as two separate emission lines. A new line mysteriously appears.
When an appropriate external field is applied the angular momentum of the particle changes in the direction of the field, ni≠noi.
This is not Zeeman effect nor Stark effect.
But an indication of the two processes involved as particles coalesce and break.
Speculating while others sleep...
The problem is n2=80 is not large enough for the various plots to be on a plateau (approaching an asymptote). Since, spectra lines are observed only in high energy conditions and we postulate that high energy conditions enables n2→large, then
RH=12πaψc
is still on the chopping block, where
ΔE2→1=h.fψc(13√n1−1(no1)2)
ΔEn→1=h.fψc(13√n1−1(no1)2)
and
ΔEn→2=h.fψc(13√n2−1(no2)2)
And in a sleep deprived and convoluted way,
ΔE2→1−ΔEn→2=h.fψc(13√n2−13√n1+1(no2)2−1(no1)2)
Which is really interesting...a transit from energy level 1 to a higher level n and a return to energy level 2. The negative sign here makes the absorption line an emission line. This is how an absorption spectrum has a parallel emission spectrum!
A collision not of basic particles but atoms that contains the basic particles. The high energy level state is achieved when the colliding atoms are close together on impact. As the atoms part after the collision, the transition ΔEn→2 occurs.
Hmmm...
n1=no1=1
where the lowest energy level coincides with the smallest particle. In general,
ni=noi=i
if we argue that given light speed a constant, angular momentum at light speed increases proportionally with the number of constituent basic particle n. This makes noi from Bohr model coincidental with ni, the number of constituent basic particles.
Which brings us to the emission plots n1=2 and n1=5,
When experimental conditions are such that ni≠noi, these two plots will split and emerge as two separate emission lines. A new line mysteriously appears.
When an appropriate external field is applied the angular momentum of the particle changes in the direction of the field, ni≠noi.
This is not Zeeman effect nor Stark effect.
But an indication of the two processes involved as particles coalesce and break.
Speculating while others sleep...
The problem is n2=80 is not large enough for the various plots to be on a plateau (approaching an asymptote). Since, spectra lines are observed only in high energy conditions and we postulate that high energy conditions enables n2→large, then
RH=12πaψc
is still on the chopping block, where
ΔE2→1=h.fψc(13√n1−1(no1)2)
ΔEn→1=h.fψc(13√n1−1(no1)2)
and
ΔEn→2=h.fψc(13√n2−1(no2)2)
And in a sleep deprived and convoluted way,
ΔE2→1−ΔEn→2=h.fψc(13√n2−13√n1+1(no2)2−1(no1)2)
Which is really interesting...a transit from energy level 1 to a higher level n and a return to energy level 2. The negative sign here makes the absorption line an emission line. This is how an absorption spectrum has a parallel emission spectrum!
A collision not of basic particles but atoms that contains the basic particles. The high energy level state is achieved when the colliding atoms are close together on impact. As the atoms part after the collision, the transition ΔEn→2 occurs.
Hmmm...
Particles In Orbits
The difference plot of the expression, 3√n2−3√n13√n1n2−n22−n21(n1n2)2
however, draws a sense of déjà vu...
The concepts leading to the expression 3√n2−3√n13√n1n2 reverses the energy sign of conventional electron energy level transitions; E1→2 is negative and the particle loses energy. E1→2 is emitted
This would make the plot for n1=1 in the above graph, an absorption line.
For all values of n2, only when n1=1 is an absorption line. The plots in black are emission lines against which we see the absorption line without direct illuminations.
Values of the plots in black below y=0 is ignored because n2≥n1.
Rydberg constant is not murdered, instead a new process is given birth.
3√n2−3√n13√n1n2 occurs at the same time as n22−n21(n1n2)2 due to quantized energy levels in Bohr model theory. The two process has reverse energy signs and hence married with a negative sign. According to Bohr model E1→2 is positive and the particle gains energy and transits to a higher energy level.
We have instead,
ΔE2→1=h.fψc(3√n2−3√n13√n1n2−n2o2−n2o1(no1no2)2)
where a change n1→n2 is accompanied by a change in orbital energy level no1→no2.
Only now are the particles in orbits.
Note: E2=E1+ΔE1→2
however, draws a sense of déjà vu...
The concepts leading to the expression 3√n2−3√n13√n1n2 reverses the energy sign of conventional electron energy level transitions; E1→2 is negative and the particle loses energy. E1→2 is emitted
This would make the plot for n1=1 in the above graph, an absorption line.
For all values of n2, only when n1=1 is an absorption line. The plots in black are emission lines against which we see the absorption line without direct illuminations.
Values of the plots in black below y=0 is ignored because n2≥n1.
Rydberg constant is not murdered, instead a new process is given birth.
3√n2−3√n13√n1n2 occurs at the same time as n22−n21(n1n2)2 due to quantized energy levels in Bohr model theory. The two process has reverse energy signs and hence married with a negative sign. According to Bohr model E1→2 is positive and the particle gains energy and transits to a higher energy level.
We have instead,
ΔE2→1=h.fψc(3√n2−3√n13√n1n2−n2o2−n2o1(no1no2)2)
where a change n1→n2 is accompanied by a change in orbital energy level no1→no2.
Only now are the particles in orbits.
Note: E2=E1+ΔE1→2
Thursday, October 13, 2016
Murder Yet Written
Of course,
3√n2−3√n13√n1n2≠1n21−1n22=n22−n21(n1n2)2
but are they parallel over the range of n1 and n2 in consideration.
A plot of 3√n2−3√n13√n1n2−n22−n21(n1n2)2 gives
where the values of the expression for n1=1 is negative and the graphs of for n1=2 and n1=5 are coincidental.
A plot of the ratio 3√n2−3√n13√n1n2n22−n21(n1n2)2 gives,
The values of the ratio varies with both n2 and n1. In the case of n1=1, the ratio 3√n2−3√n13√n1n2n22−n21(n1n2)2 is close to 1
Rydberg constant is not dead. Yet...
3√n2−3√n13√n1n2≠1n21−1n22=n22−n21(n1n2)2
but are they parallel over the range of n1 and n2 in consideration.
A plot of 3√n2−3√n13√n1n2−n22−n21(n1n2)2 gives
where the values of the expression for n1=1 is negative and the graphs of for n1=2 and n1=5 are coincidental.
A plot of the ratio 3√n2−3√n13√n1n2n22−n21(n1n2)2 gives,
The values of the ratio varies with both n2 and n1. In the case of n1=1, the ratio 3√n2−3√n13√n1n2n22−n21(n1n2)2 is close to 1
Rydberg constant is not dead. Yet...
Looking for Murder
From the previous post "" dated 13 Oct 2016,
ΔE1→2=0.2063hfψc
and so we have,
aψnew=0.2063aψ
thus assuming that the first spectra line is of double intensity, ie from the pair (n2=2,n1=1),
aψ=0.2063∗19.34=3.99nm
aψ=0.2063∗16.32=3.37nm
aψ=0.2063∗15.48=3.19nm
aψ=0.2063∗14.77=3.05nm
If, the first spectra line is the result of (nlarge,1),
aψ=0.762∗19.34=14.74nm
aψ=0.762∗16.32=12.44nm
aψ=0.762∗15.48=11.80nm
aψ=0.762∗14.77=11.25nm
ΔE1→2=0.2063hfψc
and so we have,
aψnew=0.2063aψ
thus assuming that the first spectra line is of double intensity, ie from the pair (n2=2,n1=1),
aψ=0.2063∗19.34=3.99nm
aψ=0.2063∗16.32=3.37nm
aψ=0.2063∗15.48=3.19nm
aψ=0.2063∗14.77=3.05nm
If, the first spectra line is the result of (nlarge,1),
aψ=0.762∗19.34=14.74nm
aψ=0.762∗16.32=12.44nm
aψ=0.762∗15.48=11.80nm
aψ=0.762∗14.77=11.25nm
Which is just a bunch of numbers. However, both cases point to the fact that the calculated fψ from Planck's relation, ΔE=h.fψ, is not the frequency fψc of ψ, to resonate the particle with. fψc is defined as,
fψc=cλψc=c2πaψc
where there is one wavelength m=1 around the circular path of ψ with radius aψc .
Depending on which spectra line is used to derive fψ, a factor of 0.2063 or 0.762 applies. In the case where both the double intensity emission spectra line and the first absorption spectra line are used, with the appropriate factor, there can be only one value for fψc.
Where do all these lead us?
ΔE2→1=h.fψc(3√n2−3√n13√n1n2)
The murder of Rydberg constant?
1λ2→1=RH(1n21−1n22)
Comparing the two expressions,
RH=12πaψc
which is a constant given aψc. Maybe...
Don't Worry, Be Creepy
It does not quite matter, given
f(n)=(3√n−13√n)
The value of f(n) for the range 70≤n≤79 average to
f(n)=0.762
from which we may estimate fψc from,
ΔE2→1=h.fψc(3√n2−3√n13√n13√n2)
where n1=1
from the post "Sizing Them Up Again..." dated 4 Oct 2016.
But what is n or nlarge?
Better yet since the emission spectra line as the result of (n2=2,n1=1), (two basic particles, n=1 coalesce) that produces a pair of photons, ΔE1→2 has double the intensity and hence readily identifiable,
ΔE1→2=h.fψc(3√2−3√13√13√2)
f(n)=(3√n−13√n)
n | f(n) |
---|---|
70 | 0.7573572497 |
71 | 0.758501808 |
72 | 0.7596250716 |
73 | 0.7607277244 |
74 | 0.7618104192 |
75 | 0.7628737797 |
76 | 0.7639184021 |
77 | 0.7649448568 |
78 | 0.7659536896 |
79 | 0.7669454232 |
The value of f(n) for the range 70≤n≤79 average to
f(n)=0.762
from which we may estimate fψc from,
ΔE2→1=h.fψc(3√n2−3√n13√n13√n2)
where n1=1
from the post "Sizing Them Up Again..." dated 4 Oct 2016.
But what is n or nlarge?
Better yet since the emission spectra line as the result of (n2=2,n1=1), (two basic particles, n=1 coalesce) that produces a pair of photons, ΔE1→2 has double the intensity and hence readily identifiable,
ΔE1→2=h.fψc(3√2−3√13√13√2)
where n1=1 and n2=2.
ΔE1→2=h.fψc(3√2−13√2)
ΔE1→2=0.2063hfψc
without worry about what nlarge might be.
This is different from Planck's relation E=h.f. A factor of about 15 creeps in.
Wednesday, October 12, 2016
The First Spectra Line
For the absorption spectrum where energy is measured with reference from a higher threshold, the highest energy level has the lowest drop from such a reference, we reflect the previous plot from the post "Emission Spectrum Simplified" dated 12 Oct 2016, about the axis y=0.
The first spectra line is not the line with double intensity, but
ΔE1→n=large=h.fψc(3√nlarge−3√13√13√nlarge)=h.fψc(3√nlarge−13√nlarge) --- (*)
To see what is (3√nlarge−13√nlarge), we plot
As nlarge→77, the increment in(3√nlarge−13√nlarge) decreases but the plot is not asymptotic towards a steady value around n=70≈80. (When n→∞, we have an asymptote towards y=1.)
Given that n takes on integer values (n+1 being the number of constituent basic particles the big particle has before its breakage into a basic particle (n=1) and another big particle, n), and that expression (*) at high consecutive values of n has very close values, spectra lines involving high values of n will seem to split into numerous close lines.
This could be the explanation for split spectra lines. The above is an emission spectra line plot, NOT an absorption spectra line plot.
To be sure that the first spectra line is given by (*), we look at other coalescence/breakage possibilities. When big particles of n+1, n+2 and n+3 constituent basic particles break into pairs of (n,1), (n,2) and (n,3) particles respectively,
Since the particle pairs (n=3,n+3) are at closer energy levels than (n=1,n+1), the transition from n+3 to n=3 requires less energy than the transition fro n+1 to n=1. As such breakage into a small particle of higher n involve lower absorption energy. Such lines will be higher up in the absorption spectrum plot when this plot is reflected about y=0.
After considering other possible particle pairs, (n=i,n+i), the first spectra line is still given by (*).
But how large is nlarge? nlarge=77? nlarge=74?...
The first spectra line is not the line with double intensity, but
ΔE1→n=large=h.fψc(3√nlarge−3√13√13√nlarge)=h.fψc(3√nlarge−13√nlarge) --- (*)
To see what is (3√nlarge−13√nlarge), we plot
As nlarge→77, the increment in(3√nlarge−13√nlarge) decreases but the plot is not asymptotic towards a steady value around n=70≈80. (When n→∞, we have an asymptote towards y=1.)
Given that n takes on integer values (n+1 being the number of constituent basic particles the big particle has before its breakage into a basic particle (n=1) and another big particle, n), and that expression (*) at high consecutive values of n has very close values, spectra lines involving high values of n will seem to split into numerous close lines.
This could be the explanation for split spectra lines. The above is an emission spectra line plot, NOT an absorption spectra line plot.
To be sure that the first spectra line is given by (*), we look at other coalescence/breakage possibilities. When big particles of n+1, n+2 and n+3 constituent basic particles break into pairs of (n,1), (n,2) and (n,3) particles respectively,
Since the particle pairs (n=3,n+3) are at closer energy levels than (n=1,n+1), the transition from n+3 to n=3 requires less energy than the transition fro n+1 to n=1. As such breakage into a small particle of higher n involve lower absorption energy. Such lines will be higher up in the absorption spectrum plot when this plot is reflected about y=0.
After considering other possible particle pairs, (n=i,n+i), the first spectra line is still given by (*).
But how large is nlarge? nlarge=77? nlarge=74?...
Emission Spectrum Simplified
Unfortunately in this scheme of things, we have ψ balls of various sizes, n in collisions.
When 2 particles of size n=1 coalesce 2 photons E1→2 are emitted, and when 2 particles of sizes n=1 and n=2 coalesce 2 different photons E1→3 and E2→3 are emitted.
This is not the simple scheme where emissions as the result of hops from energy level to energy level has equal intensity, but in the example above, E1→2 has twice the intensity of E1→3 and E2→3.
The plot below shows ((x+1)^(1/3)-x^(1/3))/(((x+1)*x)^1/3), ((x+2)^(1/3)-x^(1/3))/(((x+2)*x)^1/3) and ((x+3)^(1/3)-x^(1/3))/(((x+3)*x)^1/3).
where particle of size n=1, n=2 and n=3 coalesce with particle of size n=x.
We see that the highest energy transition occurs with E1→n=large, when a basic particle aψc (ie. n=1) coalesces with a large particle n→77. Two photons are released E1→n=large and Elarge→large+1.
Emission occurs in bands as n=x increases and such bands narrows with increasing n=x.
In the graph above, the top most three horizontal lines maroon, red and blue correspond to x=1. The next band of maroon, red and blue correspond to x=2. Each band progressively narrows as x increases.
As x increases, all graph approaches asymptotically to zero, ie as x increases all emissions due to the coalescence of particles of various sizes, n approaches zero.
Good night.
When 2 particles of size n=1 coalesce 2 photons E1→2 are emitted, and when 2 particles of sizes n=1 and n=2 coalesce 2 different photons E1→3 and E2→3 are emitted.
This is not the simple scheme where emissions as the result of hops from energy level to energy level has equal intensity, but in the example above, E1→2 has twice the intensity of E1→3 and E2→3.
The plot below shows ((x+1)^(1/3)-x^(1/3))/(((x+1)*x)^1/3), ((x+2)^(1/3)-x^(1/3))/(((x+2)*x)^1/3) and ((x+3)^(1/3)-x^(1/3))/(((x+3)*x)^1/3).
where particle of size n=1, n=2 and n=3 coalesce with particle of size n=x.
We see that the highest energy transition occurs with E1→n=large, when a basic particle aψc (ie. n=1) coalesces with a large particle n→77. Two photons are released E1→n=large and Elarge→large+1.
Emission occurs in bands as n=x increases and such bands narrows with increasing n=x.
In the graph above, the top most three horizontal lines maroon, red and blue correspond to x=1. The next band of maroon, red and blue correspond to x=2. Each band progressively narrows as x increases.
As x increases, all graph approaches asymptotically to zero, ie as x increases all emissions due to the coalescence of particles of various sizes, n approaches zero.
Good night.
Tuesday, October 4, 2016
Sizing Them Up Again...
With this new picture of particles coalescence and disintegration, we will calculate aψn=1 again...
From the post "No Nucleus Needed" dated 03 Oct 2016,
ΔE2→1=En1−En2=hc2πaψn1−hc2πaψn2
where positive values for ΔEn is energy absorbed. And from the post "Speculating About Spectra Series" dated 29 Sep 2016,
aψn=3√n.aψc --- (*)
where n=1,2,3,..77,
we have,
ΔE2→1=hc2π(1aψn1−1aψn2)=ℏ.c(aψn2−aψn1aψn1.aψn2)
Substitute (*) in,
ΔE2→1=ℏcaψc(3√n2−3√n13√n13√n2)
From the post "No Nucleus Needed" dated 03 Oct 2016,
ΔE2→1=En1−En2=hc2πaψn1−hc2πaψn2
where positive values for ΔEn is energy absorbed. And from the post "Speculating About Spectra Series" dated 29 Sep 2016,
aψn=3√n.aψc --- (*)
where n=1,2,3,..77,
we have,
ΔE2→1=hc2π(1aψn1−1aψn2)=ℏ.c(aψn2−aψn1aψn1.aψn2)
Substitute (*) in,
ΔE2→1=ℏcaψc(3√n2−3√n13√n13√n2)
since,
2πaψc=λψc with m=1
assuming that there is m=1 wavelength along the circular path,
ΔE2→1=h.fψc(3√n2−3√n13√n13√n2)
where fψc=cλψc.
Each possible value of ΔE2→1 due to a pair (n2,n1) of particles before and after a collision, corresponds to one spectra line. As more possible tuples of (n2,n1) are made available given the set of experimental conditions, more spectra lines appear.
Now for experimental data from the web...
Where Small is Highest
The smaller the particle the higher En is. Big particle absorb energy to break into smaller particles. When small particles coalesce energy is released as a photon that we observe as the emission spectrum.
Big particles are more susceptible to collision impacts and break into smaller particles, absorbing part of the energy of impact on breaking up. Energy is absorbed as a photon, from which we obtain the absorption spectrum.
But En is not ψ. En is the result of ψ on a circular path at light speed c.
So,
λψ≠λn
and the photon packets emitted or absorbed,
h.fvis=h.(fn1−fn2)
λvis=cfvis=cfn1−fn2
where fvis and λvis are obtained from the experimental spectrum(s) observed.
Obviously,
λvis≠λn and
λvis≠λψ
But,
λψn=λn, m=1
only when m=1 that there is one wavelength around the circular path of radius aψ. The factor 2π appears as the wavelength, λψ is wrapped around a circular path.
And since the energy transitions as particles coalesce and disintegrate is the reverse of electron energy level transitions, we do not have an issue with negative energy.
And in the rest state of no collisions, we have aψn=1 where aψ is the smallest at the highest energy possible,
En=1=Emax
aψ=aψ1=aψc
So, paradoxically ψ with aψc has the highest energy but the smallest size.
Big particles are more susceptible to collision impacts and break into smaller particles, absorbing part of the energy of impact on breaking up. Energy is absorbed as a photon, from which we obtain the absorption spectrum.
But En is not ψ. En is the result of ψ on a circular path at light speed c.
So,
λψ≠λn
and the photon packets emitted or absorbed,
h.fvis=h.(fn1−fn2)
λvis=cfvis=cfn1−fn2
where fvis and λvis are obtained from the experimental spectrum(s) observed.
Obviously,
λvis≠λn and
λvis≠λψ
But,
λψn=λn, m=1
only when m=1 that there is one wavelength around the circular path of radius aψ. The factor 2π appears as the wavelength, λψ is wrapped around a circular path.
And since the energy transitions as particles coalesce and disintegrate is the reverse of electron energy level transitions, we do not have an issue with negative energy.
And in the rest state of no collisions, we have aψn=1 where aψ is the smallest at the highest energy possible,
En=1=Emax
aψ=aψ1=aψc
So, paradoxically ψ with aψc has the highest energy but the smallest size.
Monday, October 3, 2016
No Nucleus Needed
ψ wraps around a sphere. A certain amount of energy is associated with ψ motion around the sphere. If h amount of energy is in the system, going once per second around the sphere, then travelling at light speed c around a radius of aψn, the amount of potential energy associated with this motion is,
En=h.c2πaψn
but,
2πaψn=mλm
where m is the number of wavelength, λm of ψ around the circle.
With m=1,
En=h.cλm=h.f
hm changes with m because c=fλ.
And,
hm1.f>hm2.f
when m2>m1.
When there is more wavelengths around the circular path, stored energy decreases, which suggest another way ψ can absorb and release packets of energy; by changing m. Also, given aψn at fixed value, f increases with m but hm decreases, so, En=hm.f remains a constant. f increases with decreasing aψ, with increasing En. Catastrophe when the number of particles with small aψ is also large.
En is independent of m. h is defined as one wavelength going around once per second along the circular path, then a corresponding increase in the number of wavelengths, m increases the frequency by m but this increase cancels with the decrease in h by the reciprocal of m.
With these issues with m aside, when two particles coalesce,
No nucleus needed.
En=h.c2πaψn
but,
2πaψn=mλm
where m is the number of wavelength, λm of ψ around the circle.
With m=1,
En=h.cλm=h.f
which is Planck's relation given m=1. When ψ is a half wave in time and a half wave in space space,
m=12
En=h.2cλm=2h.f=h′.f
with a mysterious factor of 2.
When m=2,3...
En=h.cmλm=hm.f=hm.f
When m=2,3...
En=h.cmλm=hm.f=hm.f
hm changes with m because c=fλ.
And,
hm1.f>hm2.f
when m2>m1.
When there is more wavelengths around the circular path, stored energy decreases, which suggest another way ψ can absorb and release packets of energy; by changing m. Also, given aψn at fixed value, f increases with m but hm decreases, so, En=hm.f remains a constant. f increases with decreasing aψ, with increasing En. Catastrophe when the number of particles with small aψ is also large.
En is independent of m. h is defined as one wavelength going around once per second along the circular path, then a corresponding increase in the number of wavelengths, m increases the frequency by m but this increase cancels with the decrease in h by the reciprocal of m.
With these issues with m aside, when two particles coalesce,
aψn1→aψn2
the bigger particle has less potential energy associated with its ψ in circular motion, The amount of energy released due to this drop in potential is.
ΔE=En1−En2=hc2πaψn1−hc2πaψn2
ΔE=hfn1−hfn2=h(fn1−fn2)
fn1>fn2
fn1>fn2
using h to denote all cases of m, as discussed above, we have an expression similar to the discrete energy level transitions expression for electrons around a nucleus, In this case, however it is just ψ alone going around a circular path and energy level decreases with increasing aψn
No nucleus needed.
Sunday, October 2, 2016
Spectra Ghost At The Rear
Happy Birthday to me...03 Oct 1968.
If spectra lines reflect the collision and subsequent coalescence of particles, then the observation that more spectra lines appear at lower experiment setup temperature, can be explained by lower collisions rate at lower temperature with less momentum which allows bigger particles to form. Bigger particles have higher aψn which appear as a higher spectra line. At higher temperature, big particles are broken up in high velocity impacts before further coalescence forms bigger particle.
So, at low temperature more spectra lines due to bigger particles appear.
Have a nice day.
If spectra lines reflect the collision and subsequent coalescence of particles, then the observation that more spectra lines appear at lower experiment setup temperature, can be explained by lower collisions rate at lower temperature with less momentum which allows bigger particles to form. Bigger particles have higher aψn which appear as a higher spectra line. At higher temperature, big particles are broken up in high velocity impacts before further coalescence forms bigger particle.
So, at low temperature more spectra lines due to bigger particles appear.
Have a nice day.
The Quantum
From the previous post "Speculating About Spectra Series" dated 29 Sep 16,
aψn=3√n.aψc
which suggests energy transition,
aψn1→aψn2
n1→n2
occurs as small particles coalesce into bigger particles and when a big particle breaks into smaller particles.
The second case explains the occurrence of two or more simultaneous energy transitions, as a bigger particle breaks into two or more smaller particles.
aψ6↗→↘aψ1aψ2aψ3
n6↗→↘n1n2n3
In the case above, a particle made up of n=6 basic particles breaks into particles of size n=1, n=2 and n=3. n denoting arbitrary energy levels before has now a physical interpretation; it is the number of constituent basic particles.
I have found the quantum! aψc is the quantum.
aψn=3√n.aψc
which suggests energy transition,
aψn1→aψn2
n1→n2
occurs as small particles coalesce into bigger particles and when a big particle breaks into smaller particles.
The second case explains the occurrence of two or more simultaneous energy transitions, as a bigger particle breaks into two or more smaller particles.
aψ6↗→↘aψ1aψ2aψ3
n6↗→↘n1n2n3
In the case above, a particle made up of n=6 basic particles breaks into particles of size n=1, n=2 and n=3. n denoting arbitrary energy levels before has now a physical interpretation; it is the number of constituent basic particles.
I have found the quantum! aψc is the quantum.